EP4069686B1 - Gpp-1-rezeptor-agonisten - Google Patents

Gpp-1-rezeptor-agonisten Download PDF

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Publication number
EP4069686B1
EP4069686B1 EP20895723.3A EP20895723A EP4069686B1 EP 4069686 B1 EP4069686 B1 EP 4069686B1 EP 20895723 A EP20895723 A EP 20895723A EP 4069686 B1 EP4069686 B1 EP 4069686B1
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Prior art keywords
benzo
imidazole
carboxylic acid
methyl
pyridin
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English (en)
French (fr)
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EP4069686C0 (de
EP4069686A4 (de
EP4069686A1 (de
Inventor
Han Kyu Lee
Jeong-Un Hwang
Kyu-Hwan Lee
Hyung-Ho Choi
Jung-In Jang
Hyuck-Joo LEE
Seung-Tae KANG
Hyun-Ho Yoon
Neul Ha
Hyun-Hwa LA
Jin Woong Kim
Dae Hoon Kim
Myoung Ki Baek
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Hyundai Pharm Co Ltd
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Hyundai Pharm Co Ltd
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/10—Radicals substituted by halogen atoms or nitro radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/12—Radicals substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • the present invention relates to a GLP-1 receptor agonist having a novel structure.
  • Diabetes is a metabolic disease which is caused by deficiency of insulin secretion or insulin action, and can be mainly classified into type 1 and type 2 depending on its mechanism.
  • Type 1 diabetes is caused by deficiency of insulin secretion resulting from autoimmune destruction of pancreatic beta cells.
  • Type 2 diabetes also referred to as insulin-independent diabetes, is mainly caused because the amount of insulin produced according to an increase in blood sugar is not sufficient for cells to absorb glucose and reduce blood sugar levels.
  • Treatment of Type 1 diabetes requires insulin therapy which involves injecting insulin externally, and for type 2 diabetes, a therapeutic agent is administrated alone or in combination, or insulin therapy is used, depending on the disease progression.
  • Insulin secretagogues are, for example, sulfonylurea (e.g., glipizide, glimepyride, glyburide), meglitinide (e.g., nateglinide, repaglinide) and dipeptidyl peptidase IV (DPP-IV) inhibitors (eg, sitagliptin, vildagliptin, alogliptin, dutogliptin, linagliptin, saxagliptin), and the like.
  • sulfonylurea e.g., glipizide, glimepyride, glyburide
  • meglitinide e.g., nateglinide, repaglinide
  • DPP-IV dipeptidyl peptidase IV
  • Biguanides are believed to act primarily to reduce the production of glucose in the liver, and the examples thereof include metformin, and the like.
  • Alpha-glucosidase inhibitors reduce the absorption of glucose in the intestine, and the examples thereof include acarbose, and the like.
  • Thiazolidinediones act on a specific receptor (peroxisome proliferator-activated receptor-gamma) in liver, muscle, and adipose tissue, and the examples thereof include pioglitazone, rosiglitazone, and the like.
  • SGLT-2 inhibitors inhibit glucose reuptake in the kidney, thereby lowering blood glucose levels, and the examples thereof include dapagliflozin, empagliflozin, canagliflozin, ertugliflozin, and the like.
  • oral diabetes medicines currently used in clinical practice cause various side effects such as hypoglycemia, diarrhea, weight gain, cardiovascular problems, liver toxicity when taken for a long time, or many of them have a limited effect.
  • insulin administration which is the last treatment method, is also inconvenient because of having to be subcutaneously injected two or three times a day, and is likely to cause hypoglycemia which is the most serious side effect.
  • GLP-1 (GLP-1) receptor agonists have recently emerged as a next generation diabetes medicine.
  • GLP-1 a long incretin hormone having 30 amino acids, is secreted by intestinal L-cells in response to ingestion of food.
  • GLP-1 plays a significant role in controlling postprandial blood glucose by promoting glucose-dependent insulin secretion in the pancreas.
  • GLP-1 also inhibits glucagon secretion, causing a decrease in hepatic glucose production.
  • GLP-1 delays gastric emptying, slows small intestine motility, and thus delays food absorption.
  • GLP-1 receptor agonists such as GLP-1 and analogs or derivatives thereof, exhibit good potential in clinical trials for the treatment of type 2 diabetes, and induces a number of biological effects such as stimulation of insulin secretion, inhibition of glucagon secretion, inhibition of gastric fasting, inhibition of gastric motility or intestinal motility, and induction of weight loss
  • GLP-1 receptor agonists provide pancreatic protection, have no risk of hypoglycemia, and maintain adequate blood sugar levels for a long time.
  • GLP-1 receptor agonists known to date include liraglutide, albiglutide, exenatide, lixisenatide, dulaglutide, semaglutide, and the like.
  • WO2018109607 discloses certain 6-carboxylic acids of benzimidazoles and 4-aza-, 5-aza-, 7-aza- and 4,7-diaza-benzimidazoles which are stated to be GLP-1 receptor agonists.
  • WO2020263695 discloses certain [[oxetan-2-yl]methyl]benzimidazole-5-carboxylic acid derivatives which are stated to be GLP-1 receptor agonists.
  • WO 2021/081207 discloses compounds, including certain 1H-benzo[d]imidazole derivatives which are stated to be GLP-1 receptor agonists.
  • WO 2022/078352 describes crystalline forms of GLP-1R agonists and uses thereof.
  • the present inventors completed the present invention by intensively investigating a GLP-1 receptor agonist having a novel structure to find that the compounds described herein have an excellent effect as a GLP-1 receptor agonist.
  • the present invention is to provide a GLP-1 receptor agonist having a novel structure.
  • the present invention provides a compound represented by the following Formula 1, or a pharmaceutically acceptable salt thereof: wherein,
  • A is phenyl; C 3-7 cycloalkyl; 5- or 6-membered heteroaryl containing one heteroatom selected from N, O, and S; or a 9- or 10-membered benzo-fused ring fused with 5- or 6-membered heteroaryl containing one or two heteroatoms selected from N, O, and S. More preferably, A is phenyl, pyrrolyl, pyridinyl, benzothiazolyl, benzoxazolyl, benzimidazolyl, cyclopropyl, or cyclobutyl. More preferably, A is phenyl, pyridinyl, benzothiazolyl, or cyclopropyl.
  • L is -(CH 2 ) n -O- or -O-(CH 2 ) n - (n is 1 or 2), and more preferably, L is - CH 2 O- or -OCH 2 -.
  • R 1 is hydrogen, C 1-5 alkyl, C 1-5 alkoxy, C 1-5 haloalkyl, halogen, cyano, or nitro
  • R 2 is hydrogen or halogen
  • R 1 is hydrogen, methyl, methoxy, trifluoromethyl, fluoro, chloro, bromo, cyano, or nitro
  • R 2 is hydrogen, fluoro, chloro, or bromo.
  • R 3 is hydrogen, fluoro, chloro, or bromo.
  • R 4 is hydrogen, C 1-5 alkyl, C 1-5 alkoxy, halogen, or nitro
  • R 5 is hydrogen or halogen.
  • R 4 is hydrogen, methyl, methoxy, fluoro, chloro, bromo, or nitro
  • R 5 is hydrogen, fluoro, chloro, or bromo.
  • R 6 is -CH 2 F; furanyl; imidazolyl unsubstituted or substituted with methyl or ethyl; oxazolyl; pyridinyl; thiophenyl; or tetrahydrofuranyl.
  • Formula 1 is represented by the following Formula 1-1: wherein
  • Formula 1 is represented by the following Formula 1-2: wherein
  • Formula 1 is represented by the following Formula 1-3: wherein
  • Formula 1 is represented by the following Formula 1-4: wherein
  • C 1-5 alkyl means a linear or branched, saturated hydrocarbon group having 1 to 5 carbon atoms.
  • a C 1-5 alkyl group includes, but is not limited to, methyl, ethyl, propyl, butyl, pentyl, 1-methylethyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, 1-methylbutyl, and 1,1-dimethylpropyl.
  • C 1-5 alkoxy is an OR group, wherein R is a C 1-5 alkyl group as defined above.
  • alkoxy group having 1 to 5 carbon atoms include, although not limited to, methoxy, ethoxy, propoxy, butoxy, 1-methylethoxy, 1,1-dimethylethoxy, 1-methylpropoxy, 2-methylpropoxy, or cyclopropylmethoxy.
  • C 1-5 haloalkyl is a C 1-5 alkyl group as defined above in which one or more hydrogen atoms are replaced by one or more halo atoms. Examples thereof include, although not limited to, a difluoromethyl or trifluoromethyl group.
  • halo is fluoro, chloro, or bromo.
  • C 3-7 cycloalkyl means a saturated hydrocarbon ring system having 3 to 7 ring carbon atoms. Examples thereof include, although not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl.
  • aryl refers to a C 6-10 aromatic group which may be substituted or unsubstituted, preferably a C 6 aryl group (i.e., phenyl).
  • heteroaryl refers to an aromatic ring system containing one or more heteroatoms selected from N, O, and S, and preferably refers to a 5- or 6-membered monocyclic aromatic ring system.
  • the 5- or 6-membered heteroaryl include, but are not limited to, pyrrolyl, thiophenyl, furanyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, imidazolyl, isoxazolyl, triazolyl, thiadiazolyl, tetrazolyl, oxadiazolyl, pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl, triazinyl, and the like.
  • fused heteroaryl refers to a ring system in which the heteroaryl group is linked with another aryl, heteroaryl, or heterocycloalkyl group in a fused way, and is preferably a 9- or 10-membered benzo-fused heteroaryl group.
  • fused heteroaryl examples include, but are not limited to, benzofuranyl, isobenzofuranyl, benzothiophenyl, indolyl, isoindolyl, indazolyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzthiazolyl, benzthiadiazolyl, benzoxadiazolyl, benztriazolyl, quinolinyl, isoquinolinyl, quinazolinyl, and the like.
  • heterocycloalkyl refers to a saturated or partially unsaturated ring system containing one or more heteroatoms selected from N, O, and S, and is preferably 4-, 5- or 6-membered heterocycloalkyl.
  • heterocycloalkyl include, but are not limited to, oxiranyl, aziridinyl, azetidinyl, oxetanyl, tetrahydrofuranyl, tetrahydrothiophenyl, pyrrolidinyl, 3-pyrrolinyl, 2-pyrrolinyl, 2H-pyrrolyl, 1H-pyrrolyl, imidazolidinyl, 2-imidazolinyl, pyrazolidinyl, 2-pyrazolinyl, oxazolidinyl, isoxazolidinyl, isothiazolidinyl, thiazolidinyl, oxadiazolidinyl, thiadiazolidinyl,
  • a compound of the present invention may exist in the form of a salt, particularly a pharmaceutically acceptable salt.
  • the pharmaceutically acceptable salt is a metal salt, more preferably a salt of sodium, potassium, cesium, lithium, magnesium, or calcium.
  • the metal salt may be prepared using an inorganic base or an organic base.
  • the compound represented by Formula 1 is dissolved in a water-miscible organic solvent, such as acetone, methanol, ethanol, or acetonitrile, thereafter an organic base or an inorganic base is added thereto, and then precipitated crystals are prepared through filtration, and dried, thereby obtaining a pharmaceutically acceptable salt.
  • the pharmaceutically acceptable salt may be prepared by vacuuming the solvent from a reaction mixture with a base added thereinto, followed by drying the residue, or by adding another organic solvent and filtering the precipitated salt.
  • the corresponding salt is obtained by reacting an alkali metal or alkaline earth metal salt with a suitable silver salt (e.g., silver nitrate).
  • the salt may be prepared using various organic bases as well as metal salts, and typically, tris salts may be prepared using tris(hydroxymethyl)aminomethane.
  • a pharmaceutically acceptable salt may be prepared using a basic amino acid.
  • the amino acid salt it is pharmaceutically suitable to prepare a natural amino acid salt such as arginine, histamine, and lysine.
  • a pharmaceutically unacceptable salt or solvate of the compound represented by Formula 1 may be used as an intermediate in the preparation of the compound represented by Formula 1, or a pharmaceutically acceptable salt or solvate thereof.
  • the compound represented by Formula 1 of the present invention includes not only a pharmaceutically acceptable salt thereof, but also all possible solvates and hydrates that may be prepared therefrom, and includes all possible stereoisomers as well. Solvates, hydrates, and stereoisomers of the compound represented by Formula 1 may be prepared and used from the compound represented by Formula 1 using conventional methods.
  • the compound represented by Formula 1 according to the present invention may be prepared in a crystalline or amorphous form.
  • the compound represented by Formula 1 may be optionally hydrated or solvated when prepared in a crystalline form.
  • the present invention may include stoichiometric hydrates of the compounds represented by Formula 1 as well as compounds containing various amounts of water.
  • Solvates of the compound represented by Formula 1 according to the present invention include both stoichiometric solvates and non-stoichiometric solvates.
  • the compound represented by Formula 1 may be prepared using a preparation method as shown in Reaction Scheme 1 below.
  • Step 1-1 is a Suzuki coupling reaction, in which a compound represented by Formula C is prepared by reacting a compound represented by Formula A with a compound represented by Formula B. It is preferable to carry out the reaction in the presence of a palladium catalyst and a base, and a reactor for the Suzuki coupling reaction may be modified in accordance with the common knowledge in the art.
  • Step 1-2 is a hydrolysis reaction, in which a methyl ester group (or ethyl ester group) is converted into a carboxyl group. It is preferable to carry out the reaction in the presence of a base, and the reaction conditions for the hydrolysis reaction can be applied in accordance with the common knowledge in the art.
  • the preparation method of Reaction Scheme 1 may be more specified in Examples to be described later.
  • a compound represented by Formula 1 may be prepared using a preparation method shown in Reaction Scheme 2 below.
  • Step 2-1 is a Suzuki coupling reaction, in which a compound represented by Formula E is prepared by reacting a compound represented by Formula A with a compound represented by Formula D. It is preferable to carry out the reaction in the presence of a palladium catalyst and a base, and a reactor for the Suzuki coupling reaction may be modified in accordance with the common knowledge in the art.
  • Step 2-2 is a hydrolysis reaction, in which a methyl ester group (or ethyl ester group) is converted into a carboxyl group.
  • the reaction is preferably carried out in the presence of a base, and the reaction conditions for the hydrolysis reaction can be applied in accordance with the common knowledge in the art.
  • Step 2-3 is an amidation reaction, in which a compound represented by Formula H is prepared by reacting a compound represented by Formula F with a compound represented by Formula D.
  • the reaction conditions for the amidation reaction can be applied in accordance with the common knowledge in the art.
  • Step 2-4 is a cyclization reaction, in which a compound represented by Formula H is reacted under acidic conditions to form a benzoimidazole ring.
  • the reaction conditions for the cyclization reaction can be applied in accordance with the common knowledge in the art.
  • Step 2-5 is a hydrolysis reaction, in which a methyl ester group (or ethyl ester group) is converted into a carboxyl group. It is preferable to carry out the reaction in the presence of a base, and the reaction conditions for the hydrolysis reaction can be applied in accordance with the common knowledge in the art.
  • the preparation method of Reaction Scheme 2 may be more specified in Examples to be described later.
  • the present invention provides a pharmaceutical composition for use in preventing or treating a disease associated with GLP-1 activity, which contains, as an active ingredient, a compound represented by Formula 1, or a pharmaceutically acceptable salt, hydrate, solvate or isomer thereof.
  • the compound represented by Formula 1, or a pharmaceutically acceptable salt, hydrate, solvate, or isomer thereof, which is a GLP-1 receptor agonist induces effects such as stimulation of insulin secretion, inhibition of glucagon secretion, inhibition of gastric fasting, inhibition of gastric motility or intestinal motility, and induction of weight loss, and may thus be usefully used for preventing or treating a disease associated with GLP-1 activity.
  • Examples of the disease associated with GLP-1 activity include diabetes, hyperglycemia, insulin resistance, impaired glucose tolerance, diabetic neuropathy, diabetic nephropathy, obesity, glucose metabolism disorder, hyperlipidemia, dyslipidemia, cardiovascular disease, arteriosclerosis, non-alcoholic fatty liver disease, or non-alcoholic steatohepatitis.
  • prevention means any action that inhibits or delays the development, spread, and recurrence of the disease by administration of the pharmaceutical composition of the present invention
  • treatment means any action that alleviates or advantageously alters the symptoms of the disease by administration of the pharmaceutical composition of the present invention.
  • compositions of the present invention may be formulated in oral or parenteral dosage form according to the standard pharmaceutical practice. These formulations may contain additives such as a pharmaceutically acceptable carrier, an adjuvant, or a diluent, in addition to the active ingredient.
  • the carrier suitably includes, although not limited to, for example, physiological saline, polyethylene glycol, ethanol, vegetable oil and isopropylmyristate and the like
  • the diluent suitably includes, although not limited to, lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and/or glycine, etc.
  • the compounds of the present invention can be dissolved in oil, propylene glycol, or other solvents commonly used in the preparation of injectable solutions. Further, the compounds of the present invention may be formulated as ointments or creams for topical effects.
  • the pharmaceutical dosage form of the compounds according to the present invention may be used in the form of a pharmaceutically acceptable salt or solvate thereof, and may also be used alone or in combination with other pharmaceutically active compounds, as well as in a suitable set.
  • the compounds of the present invention may be dissolved, suspended or emulsified in a general saline, a water-soluble solvent such as 5% dextrose, or a non-water-soluble solvent such as synthetic fatty acid glyceride, higher fatty acid ester or propylene glycol to be formulated as an injection.
  • the formulation of the present invention may include conventional additives such as solubilizers, isotonic agents, suspending agents, emulsifiers, stabilizers, and preservatives.
  • the preferred dosage of the compound according to the present invention varies depending on the condition and weight of the patient, the extent of the disease, the form of the therapeutic agent, the route and duration of administration, but may be appropriately selected by those skilled in the art.
  • the compound of the present invention may be administered at 0.0001 to 100 mg/kg (body weight), preferably 0.001 to 100 mg/kg (body weight) per day.
  • the compound may be administered once a day or in divided doses via an oral or parenteral route.
  • the composition may contain 0.001 to 99 wt.%, preferably 0.01 to 60 wt.% of the compound of the present invention.
  • the pharmaceutical composition of the present invention may be administered to mammals including rats, mice, livestock, and humans by various routes. All administration methods can be envisaged, and the composition may be administered, for example, by oral, rectal or intravenous, intramuscular, subcutaneous, intrauterine dural or intracerebroventricular injection
  • a compound according to the present invention may be usefully used as a GLP-1 receptor agonist for use in preventing or treating a disease associated with GLP-1 activity.
  • reaction mixture was concentrated under reduced pressure, and extracted with ethyl acetate (40 mL) and distilled water (20 mL) to separate an organic layer. After separation, the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. Thereafter, separation was performed using column chromatography under the condition of ethyl acetate: n-hexane (1:5 (volume ratio)). The resulting compound was concentrated under reduced pressure, thereby obtaining a target compound (0.158 g, 0.26 mmol, yield: 22.09%).
  • the reaction product was concentrated under reduced pressure, and then distilled water (30 mL) was added, followed by extraction with ethyl acetate (50 mL). The extracted organic layer was dried over anhydrous magnesium sulfate and filtered under reduced pressure. The filtered solution was concentrated under reduced pressure, and then separated by a column, thereby obtaining a target compound (4.7 g, yield: 73%).
  • methyl 2-(4-(6-((4-chloro-2-fluorobenzyl)oxy)pyridin-2-yl)-3-fluorophenyl)acetate (3 g, 7.43 mmol) prepared in step 2 was dissolved in methanol (15 mL) and distilled water (15 mL), and then 2N potassium hydroxide aqueous solution (3 mL) was added, followed by stirring for 8 hours at room temperature.
  • the reaction product was concentrated under reduced pressure, and then 1N hydrochloric acid aqueous solution (8 mL) was added, followed by extraction with distilled water (20 mL) and ethyl acetate (30 mL).
  • the extracted organic layer was washed twice with saturated sodium hydrogen carbonate aqueous solution (50 mL), and the organic layer was separated. The separated organic layer was dried over anhydrous magnesium sulfate and then filtered under reduced pressure. The filtered solution was concentrated under reduced pressure, ethyl acetate (10 mL) was added, and then n-hexane (30 mL) was added, followed by stirring for 30 minutes. The resulting solid was filtered with n-hexane solution, thereby obtaining a target compound (2.71 g, yield: 92%).
  • the reaction product was concentrated under reduced pressure, and then 1N hydrochloric acid aqueous solution (3 mL) was added, followed by extraction with distilled water (10 mL) and ethyl acetate (15 mL). The extracted organic layer was dried over anhydrous magnesium sulfate and filtered under reduced pressure. The filtered solution was concentrated under reduced pressure, and the resulting solid was filtered with n-hexane solution, thereby obtaining a target compound (742 mg, yield: 76%).
  • 2-bromo-6-((4-chloro-2-fluorobenzyl)oxy)pyridine (780 mg, 2.5 mmol) previously prepared in step 1 and 2-((4-methoxybenzyl)oxy)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (870 mg, 2.55 mmol) were dissolved in tetrahydrofuran: distilled water: methanol (4:2:1 (volume ratio); 20 mL, 10 mL, 5 mL; total 35 mL).
  • Lithium hydroxide (152 mg, 3.62 mmol) was added at room temperature, and then stirred at room temperature for 12 hours. After completion of the reaction, the reaction product was neutralized to a pH of 6-7 with 1N hydrochloric acid aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, followed by filtration, and distilled under reduced pressure. The solvent was removed, and then the residue was solidified with ethyl acetate, thereby obtaining a target compound (480 mg, yield: 70%).
  • Example 1-6 The following Examples 1-6, 8-59, and 61-103 were prepared in the same manner as in Example 60, except that suitable starting materials were used according to the structure of the compound to be prepared.
  • Examples 104 to 109, 111 and 112 below were prepared in the same manner as in Example 110, except that starting materials according to the structure of the compound to be prepared were used.
  • Example 104 Preparation of 2-((4-(3-(4-cyano-2-fluorobenzyloxy)phenyl)-2-oxopyridin-1(2H)-yl)methyl)-1-(2-methoxyethyl)-1H-benzo [d] imidazole-6-carboxylic acid
  • Example 105 Preparation of 2-((4-(6-(4-chloro-2-fluorobenzyloxy)pyridin-2-yl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazole-6-carboxylic acid
  • Example 106 Preparation of 2-((4-(3-(4-chloro-2-fluorobenzyloxy)phenyl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazole-6-carboxylic acid
  • Examples 113 to 130 and 132 to 135 below were prepared in the same manner as in Example 60, except that starting materials according to the structure of the compound to be prepared were used.
  • the efficacy of the compound according to the present invention as a GLP-1 receptor agonist was determined by measuring cAMP (cyclic Adenosine Monophosphate) activity using a CHO-K1/GLP-1 receptor-expressing cell (Genscript, M00451) that expresses a human GLP-1 receptor.
  • cAMP cyclic Adenosine Monophosphate
  • CHO-K1/GLP1 receptor-expressing cells in a Ham's F12 medium containing 10% FBS, 1% NEAA, 200 ug/ml Zeocin, and 100 ug/ml Hygromycin B were dispensed into a 96-well plate (SPL, 30096) at the amount of 30,000 cells/100 uL/well, and incubated in a 37°C, 5% CO 2 incubator. The next day, the medium was removed, and a 50 uL of HBSS medium containing 0.1% BSA, 0.5 mM IBMX, and 5 mM HEPES was added to each well.
  • test substance (6.4 nM to 20 uM) of 2X concentration in the HBSS medium containing 0.1% BSA, 0.5 mM IBMX, and 5 mM HEPES
  • 50 uL of the HBSS medium in which the test substance was dissolved was added to each well, and incubated in a 37°C, 5% CO 2 incubator.
  • the cAMP activity was measured according to the manufacturer's instructions using the cAMP dynamic HTRF kit (Cisbio, 62AM4PEC). After incubation, the medium was discarded, and the cells were lysed. cAMP-d2 and anti-cAMP cryptate conjugate were added thereto and reacted for 3 hours.
  • FRET fluorescence resonance energy transfer
  • Intracellular cAMP competes with cAMP-d2 for anti-cAMP cryptate, and the measured signal of fluorescence resonance energy transfer (FRET) is inversely proportional to intracellular cAMP.
  • EC 50 10 nM 31 3200 nM 61 8.7 nM 91 7.2 nM 121 15 nM 2 63 nM 32 32 nM 62 37 nM 92 78 nM 122 9.5 nM 3 32 nM 33 60 nM 63 160 nM 93 1100 nM 123 14 nM 4 200 nM 34 9.2 nM 64 110 nM 94 1.3 nM 124 4.3 nM 5 620 nM 35 9.0 nM 65 5 nM 95 100 nM 125 37 nM 6 25 nM 36 88 nM 66 4.6 nM 96 830 nM 126 510 nM 7 2000 nM 37 13 nM 67 11 nM 97 31 nM 127 20 nM 8 120 nM 38* 140 nM 68 29 nM 98 61 nM 128 260 nM 9 75 nM 39 250 nM 69
  • hERG Human ether-a-go-go-related gene
  • test substance was dissolved in DMSO to prepare a 50 mM solution.
  • a 4 mM solution was prepared by diluting the 50 mM solution with DMSO in a U bottom 96-well plate (SPL, 34096), and was then diluted 100-fold with a test buffer to prepare a 40 uM (4X) solution.
  • the positive control E-4031 (3 mM) provided in the kit was diluted 25-fold with a test buffer to prepare a 120 uM solution. 5 uL of the diluted test substance solution was dispensed into a 384-well assay plate (corning, 3677).
  • hERG Membrane (2X) and Tracer (4X) provided in the kit were respectively added at 10 uL and 5 uL, and then subjected to the reaction at room temperature for 2.5 hours. After completion of the reaction, fluorescence polarization (mP) was measured with a Multimode Plate Reader (Perkin-Elmer, Envision) (excitation wavelength of 531 nm, and emission wavelength 579 nm).
  • CYP inhibition was tested to confirm the effects of the compounds according to the present invention on liver metabolic enzymes.
  • Corning (459500, 459400, 459100) kits were used for CYP1A2, CYP2C19, and CYP3A4, and Invitrogen (P2861, P2862) kits were used for CYP2C9 and CYP2D6, and the test method basically followed the test methods of each manufacturer.
  • the test compound was initially prepared by diluting the compound in DMSO (Sigma, 276855) to have a concentration of 50 mM.
  • the test compound 50 mM
  • the test compound was diluted in acetonitrile to have a concentration of 50X of a final concentration (10 uM), and a NADPH-coenzyme mixture and an enzyme-substrate mixture were mixed at a predetermined concentration provided by the kit, according to the type of enzyme.
  • 4 uL of the 50X test compound and 96 uL of the NADPH-coenzyme mixture were mixed in the U-bottom 96-well plate, and then reacted first in a 37°C incubator for 10 minutes.
  • test compound 50 mM was diluted in a test buffer to have a concentration of 2.5X of a final concentration (10 uM).
  • the enzyme mixture and the substrate mixture were mixed at a predetermined concentration provided by the kit, according to the type of enzyme. 80 uL of the 2.5X test compound prepared in the U-bottom 96-well plate and 100 uL of the enzyme mixture were mixed, reacted first for 10 minutes. Then, 20 uL of the substrate mixture was added thereto and reacted for 1 hour.
  • the reaction product was transferred to a white plate and the fluorescence wavelength was read by a microplate reader (Molecular Device, Flexstation 3) (for CYP2C9, excitation wavelength of 415 nm, emission wavelength of 460 nm; for CYP2D6, excitation wavelength of 415 nm, emission wavelength of 520 nm).
  • CYP inhibition (remaining activity % at 10 uM) CYP1A2 CYP2C9 CYP2C19 CYP2D6 CYP3A4 31 99.80 12.37 84.45 93.84 110.98 32 75.90 19.82 27.84 67.67 81.70 33 89.21 16.02 27.81 69.76 81.27 34 98.60 23.52 29.56 66.89 73.69 35 84.53 42.43 27.88 60.39 54.98 36 110.17 31.58 35.70 84.11 83.81 37 107.89 41.87 46.15 93.81 88.84 38* 99.95 32.85 49.46 72.59 83.26 39 100.04 11.46 52.62 80.38 88.18 40 100.49 13.68 39.58 78.41 81.97 41 108.66 20.65 56.87 86.19 88.63 42 100.63 15.41 79.56 87.
  • CYP inhibition (remaining activity % at 10 uM) CYP1A2 CYP2C9 CYP2C19 CYP2D6 CYP3A4 61 112.00 28.79 51.87 96.84 78.96 62 100.27 38.89 47.82 91.61 91.92 63 110.74 81.33 77.69 98.65 100.06 64 109.09 48.48 65.16 81.39 95.70 65 75.99 42.76 53.28 93.74 90.75 66 102.99 57.88 61.59 94.24 90.23 67 99.54 63.02 90.18 96.78 94.17 68 100.92 52.81 62.76 89.37 82.38 69 104.00 53.70 61.32 89.90 80.80 70 107.36 45.49 73.46 97.43 96.67 71 96.64 34.49 45.33 88.89
  • CYP inhibition (remaining activity % at 10 uM) CYP1A2 CYP2C9 CYP2C19 CYP2D6 CYP3A4 91 71.41 54.70 84.89 91.07 82.39 92 89.26 23.19 59.43 90.93 84.39 93 99.48 12.77 64.82 91.30 96.89 94 107.24 21.50 52.42 83.59 74.71 95 109.31 15.52 54.19 86.41 89.42 96 99.04 22.28 76.26 90.36 83.45 97 111.22 16.35 49.74 87.71 76.63 98 114.47 24.09 65.18 92.76 66.06 99 107.41 18.08 47.66 85.68 79.18 100 106.59 15.97 58.10 91.44 81.71 101 102.61 41.54 73.00 95.03 86
  • CYP inhibition (remaining activity % at 10 uM) CYP1A2 CYP2C9 CYP2C19 CYP2D6 CYP3A4 121 106.63 14.48 41.57 87.03 108.67 122 102.25 20.08 77.57 87.86 86.20 123 107.73 24.34 49.67 97.41 111.65 124 99.82 36.23 32.31 94.52 104.43 125 105.68 48.25 93.59 106.95 105.69 126 105.07 71.05 88.48 99.82 105.90 127 96.13 68.21 94.03 93.45 94.15 128 83.49 63.11 87.55 77.61 29.34 129 95.24 84.59 100.56 95.8 44.29 130 97.75 52.88 85.28 90.98 87.47 131 99.90 54.

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Claims (16)

  1. Verbindung, dargestellt durch die folgende Formel 1, oder pharmazeutisch annehmbares Salz davon:
    Figure imgb0169
     wobei
    A C6-10-Aryl; C3-7-Cycloalkyl; 5- oder 6-gliedriges Heteroaryl enthaltend ein Heteroatom ausgewählt aus N, O und S; 5- oder 6-gliedriges Heterocycloalkyl enthaltend ein Heteroatom ausgewählt aus N, O und S; oder 9- oder 10-gliedriges kondensiertes Heteroaryl enthaltend zumindest ein Heteroatom ausgewählt aus N, O und S ist,
    B ein beliebiges der folgenden (1) bis (5) ist,
    Figure imgb0170
    L -(CH2)n-O-, -O-(CH2)n-, -(CH2)n-NH-, -NH-(CH2)n-, -(CH2)n-N(C1-5-Alkyl)-, -N(C1-5-Alkyl)-(CH2)n-, -CONH- oder -NHCO- ist, wobei n 1 oder 2 ist,
    X CH oder N ist,
    R1 und R2 jeweils unabhängig ausgewählt sind aus der Gruppe bestehend aus Wasserstoff, C1-5-Alkyl, C1-5-Alkoxy, Ci-s-Haloalkyl, Halogen, Cyano und Nitro,
    R3 Wasserstoff oder Halogen ist,
    R4 und R5 jeweils unabhängig ausgewählt sind aus der Gruppe bestehend aus Wasserstoff, C1-5-Alkyl, C1-5-Alkoxy, C1-5-Haloalkyl, Halogen, Cyano und Nitro,
    R6 -CH2F; Furanyl; Imidazolyl unsubstituiert oder substituiert mit Methyl oder Ethyl; Oxazolyl; Pyridinyl; Thiophenyl; oder Tetrahydrofuranyl ist.
  2. Verbindung nach Anspruch 1 oder pharmazeutisch annehmbares Salz davon, wobei:
    A C6-10-Aryl; C3-6-Cycloalkyl; 5- oder 6-gliedriges Heteroaryl enthaltend ein Heteroatom ausgewählt aus N, O und S; 5- oder 6-gliedriges Heterocycloalkyl enthaltend ein Heteroatom ausgewählt aus N, O und S; oder 9- oder 10-gliedriges kondensiertes Heteroaryl enthaltend zumindest ein Heteroatom ausgewählt aus N, O und S ist,
    R2 Wasserstoff oder Halogen ist,
    R4 Wasserstoff, C1-5-Alkyl, Ci-s-Alkoxy, Halogen oder Nitro ist,
    R5 Wasserstoff oder Halogen ist, und
    B, L, X, R1, R3 und R6 wie in Anspruch 1 definiert sind.
  3. Verbindung nach Anspruch 1 oder pharmazeutisch annehmbares Salz davon, wobei A Phenyl, Pyridinyl, Benzothiazolyl oder Cyclopropyl ist.
  4. Verbindung nach Anspruch 1 oder Anspruch 3 oder pharmazeutisch annehmbares Salz davon, wobei L -CH2O- oder -OCH2- ist.
  5. Verbindung nach Anspruch 1 oder pharmazeutisch annehmbares Salz davon, wobei R1 Wasserstoff, Methyl, Methoxy, Trifluormethyl, Fluor, Chlor, Brom, Cyano oder Nitro ist.
  6. Verbindung nach Anspruch 1 oder pharmazeutisch annehmbares Salz davon, wobei R2 Wasserstoff, Fluor, Chlor oder Brom ist.
  7. Verbindung nach Anspruch 1 oder pharmazeutisch annehmbares Salz davon, wobei R4 Wasserstoff, Methyl, Methoxy, Fluor, Chlor, Brom oder Nitro ist.
  8. Verbindung nach Anspruch 1 oder pharmazeutisch annehmbares Salz davon, wobei R5 Wasserstoff, Fluor, Chlor oder Brom ist.
  9. Verbindung nach einem der Ansprüche 1 bis 4, wobei die Verbindung dargestellt ist durch die folgende Formel 1-1:
    Figure imgb0171
    Figure imgb0172
    oder pharmazeutisch annehmbares Salz davon,
    wobei Y CH oder N ist;
    wobei optional:
    (i) R1 Wasserstoff, Methyl, Methoxy, Trifluormethyl, Fluor, Chlor, Brom, Cyano oder Nitro ist und R2 Wasserstoff, Fluor, Chlor oder Brom ist; und/oder
    (ii) R4 Wasserstoff, Methyl, Methoxy, Fluor, Chlor, Brom oder Nitro ist und R5 Wasserstoff, Fluor, Chlor oder Brom ist.
  10. Verbindung nach Anspruch 1, wobei die Verbindung dargestellt ist durch die folgende Formel 1-2:
    Figure imgb0173
    oder pharmazeutisch annehmbares Salz davon,
    wobei Y CH oder N ist;
    wobei optional:
    (i) R1 Wasserstoff, Methyl, Methoxy, Trifluormethyl, Fluor, Chlor, Brom, Cyano oder Nitro ist und R2 Wasserstoff, Fluor, Chlor oder Brom ist; und/oder
    (ii) R4 Wasserstoff, Methyl, Methoxy, Fluor, Chlor, Brom oder Nitro ist und R5 Wasserstoff, Fluor, Chlor oder Brom ist.
  11. Verbindung nach einem der Ansprüche 1 bis 4, wobei die Verbindung dargestellt ist durch die folgende Formel 1-3:
    Figure imgb0174
    oder pharmazeutisch annehmbares Salz davon,
    wobei Z CH oder N ist;
    wobei optional R1 Wasserstoff, Methyl, Methoxy, Trifluormethyl, Fluor, Chlor, Brom, Cyano oder Nitro ist und R2 Wasserstoff, Fluor, Chlor oder Brom ist.
  12. Verbindung nach Anspruch 1, wobei die Verbindung dargestellt ist durch die folgende Formel 1-4:
    Figure imgb0175
    oder pharmazeutisch annehmbares Salz davon,
    wobei Z CH oder N ist;
    wobei optional R1 Wasserstoff, Methyl, Methoxy, Trifluormethyl, Fluor, Chlor, Brom, Cyano oder Nitro ist und R2 Wasserstoff, Fluor, Chlor oder Brom ist.
  13. Verbindung nach einem der Ansprüche 1 bis 4 oder 9 bis 12 oder pharmazeutisch annehmbares Salz davon, wobei R3 Wasserstoff, Fluor, Chlor oder Brom ist.
  14. Verbindung nach Anspruch 1, wobei die Verbindung ausgewählt ist aus der Gruppe bestehend aus:
    1) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)benzyl)-1-(pyridin-3-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    8) 2-((3'-(4-Cyano-2-fluorbenzyloxy)biphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    9) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-2-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    10) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    11) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    12) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)benzyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    13) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    14) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    15) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    16) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    17) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    18) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)benzyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    19) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    23) 1-(Furan-2-ylmethyl)-2-((5-(3-(3-methoxybenzyloxy)phenyl)pyridin-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    24) 2-((3'-(4-Chlor-2-fluorbenzyloxy)biphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    27) 2-((3'-(4-Cyano-2-fluorbenzyloxy)biphenyl-4-yl)methyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    28) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    29) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-2-methylbiphenyl-4-yl)methyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    30) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-3-methylbenzyl)-1-(furan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    32) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-(oxazol-5-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    33) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-2-fluorbiphenyl-4-yl)methyl)-1-(oxazol-5-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    34) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(oxazol-5-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    35) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3 -fluorbenzyl)-1-(oxazol-5-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    41) (R)-2-((3'-(4-Chlor-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    42) (R)-2-((3'-(4-Chlor-2-fluorbenzyloxy)-2-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    43) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(2-fluorethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    44) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(2-fluorethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    45) (R)-2-(4-(6-((4-Chlor-2-fluorphenoxy)methyl)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    46) (R)-2-((3'-(4-Cyano-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    47) (R)-2-((3'-(4-Cyano-2-fluorbenzyloxy)-2-fluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    49) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    50) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    51) (R)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    52) (R)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    55) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-(2-fluorethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    56) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-(2-fluorethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    57) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-(2-fluorethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    58) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-(2-fluorethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    59) (S)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    60) (S)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    61) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,3-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    62) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2,3-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    63) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-methoxybenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    64) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-methoxybenzyl)-1 - ((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    65) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,6-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    66) (S)-2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1 - ((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    67) (S)-2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    68) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-methylbenzyl)-1 - ((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    69) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-methylbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    70) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,5-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    71) 2-(4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2,5-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    72) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((1-ethyl-1H-imidazol-5-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    75) 2-(4-(6-(4-Chlorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    76) 2-(2-Fluor-4-(6-(4-methylbenzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    77) 2-(2-Fluor-4-(6-(4-(trifluormethyl)benzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    80) 2-(2-Fluor-4-(6-(3-methylbenzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    81) 2-(2-Fluor-4-(6-(3-methoxybenzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    83) 2-(4-(6-(Benzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    85) 2-(4-(6-(3,4-Difluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    87) 2-(4-(6-(4-Cyanobenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    88) 2-(2-Fluor-4-(6-(4-nitrobenzyloxy)pyridin-2-yl)benzyl)-1 -((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    89) 2-(4-(6-(4-Brom-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    90) 2-(3-Fluor-4-(6-(3-methylbenzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    91) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)-5-fluorpyridin-2-yl)-2-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    92) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-2,4'-difluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    93) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-2,4'-difluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    94) 2-(4-(6-(4-Chlorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    95) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-3,4'-difluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    96) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-3,4'-difluorbiphenyl-4-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    97) 2-(3-Fluor-4-(6-(4-(trifluormethyl)benzyloxy)pyridin-2-yl)benzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    98) 2-(4-(6-(3,4-Difluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    99) 2-(4-(6-(4-Chlor-3 -fluorbenzyloxy)pyridin-2-yl)-3 -fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    100) 2-(4-(6-(3-Chlor-5-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    101) 2-(4-(6-(2-Chlor-6-fluorbenzyloxy)pyridin-2-yl)-3 -fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    102) 2-((5-(3-(4-Chlor-2-fluorbenzyloxy)-4-fluorphenyl)pyridin-2-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    105) 2-((4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    106) 2-((4-(3-(4-Chlor-2-fluorbenzyloxy)phenyl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    107) 2-((4-(3-(4-Cyano-2-fluorbenzyloxy)phenyl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    108) (S)-2-((4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    109) (S)-2-((4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-oxopyridin-1(2H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    112) 2-((4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-6-oxopyrimidin-1(6H)-yl)methyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    116) (S)-2-(4-(6-((4-Chlor-2-fluorbenzyl)oxy)pyridin-2-yl)-2,5-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    120) (S)-2-(4-(6-((4-Cyano-2-fluorbenzyl)oxy)pyridin-2-yl)-2,5-difluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure, und
    130) 2-(4-(6-((4-Cyano-2-fluorbenzyl)oxy)pyridin-2-yl)-3-fluorbenzyl)-1-((tetrahydrofuran-2-yl)methyl)-1H-benzo[d]imidazol-6-carbonsäure,
    oder pharmazeutisch annehmbares Salz davon.
  15. Verbindung, ausgewählt aus der Gruppe bestehend aus:
    2) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)benzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    3) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-fluorbenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    4) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-methylbenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    5) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-nitrobenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    6) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-3-fluorbenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    7) 2-(4-(6-((4-Chlor-2-fluorphenoxy)methyl)pyridin-2-yl)-2-nitrobenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    21) 2-((3'-(4-Cyano-2-fluorbenzyloxy)biphenyl-4-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    22) 2-((3'-(4-Chlor-2-fluorbenzyloxy)biphenyl-4-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    31) 2-(4-(6-((4-Chlor-2-fluorphenoxy)methyl)pyridin-2-yl)-2-fluorbenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    36) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-3-fluorbiphenyl-4-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    37) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,6-difluorbenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    39) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-2-fluorbiphenyl-4-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    40) 2-((3'-(4-Cyano-2-fluorbenzyloxy)-2-fluorbiphenyl-4-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    48) 2-((3'-(4-Chlor-2-fluorbenzyloxy)-3,5-difluorbiphenyl-4-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    53) 2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2-methylbenzyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    82) (S)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,3-difluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    84) (S)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,6-difluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    86) (S)-2-(4-(6-(4-Chlor-2-fluorbenzyloxy)pyridin-2-yl)-2,5-difluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    104) 2-((4-(3-(4-Cyano-2-fluorbenzyloxy)phenyl)-2-oxopyridin-1(2H)-yl)methyl)-1-(2-methoxyethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    110) (S)-2-((6-((4-Chlor-2-fluorbenzyl)oxy)-2'-oxo-[2,4'-bipyridin]-1'(2'H)-yl)methyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    111) (S)-2-((4-(6-(4-Cyano-2-fluorbenzyloxy)pyridin-2-yl)-2-oxopyridin-1(2H)-yl)methyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    113) (S)-2-(4-(6-((4-Cyano-2-fluorbenzyl)oxy)pyridin-2-yl)-2,3-difluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    115) (S)-2-(4-(6-((4-Cyano-2-fluorbenzyl)oxy)pyridin-2-yl)-2,5-difluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    118) (S)-2-(4-(6-((4-Cyanobenzyl)oxy)pyridin-2-yl)-3-fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    119) (S)-2-(4-(6-((2,4-Difluorbenzyl)oxy)pyridin-2-yl)-3-fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    121) (S)-2-(3-Fluor-4-(6-((4-(trifluormethyl)benzyl)oxy)pyridin-2-yl)benzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    122) (S)-2-(3-Fluor-4-(6-((4-methoxybenzyl)oxy)pyridin-2-yl)benzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    123) (S)-2-(4-(6-((4-Chlorbenzyl)oxy)pyridin-2-yl)-3-fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    124) (S)-2-(3-Fluor-4-(6-((4-nitrobenzyl)oxy)pyridin-2-yl)benzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    125) (S)-2-(4-(6-((3,4-Difluorbenzyl)oxy)pyridin-2-yl)-3-fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    126) (S)-2-(4-(6-((2-Chlor-6-fluorbenzyl)oxy)pyridin-2-yl)-3-fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    127) 2-((6-((4-Chlor-2-fluorbenzyl)oxy)-2'-oxo-[2,4'-bipyridin]-1'(2'H)-yl)methyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    128) (S)-2-(3-Fluor-4-(6-(pyridin-4-ylmethoxy)pyridin-2-yl)benzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    129) (S)-2-(3-Fluor-4-(6-(pyridin-3-ylmethoxy)pyridin-2-yl)benzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    131) (S)-2-((4-(6-((4-Chlor-2-fluorbenzyl)oxy)pyridin-2-yl)-1H-pyrazol-1-yl)methyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    132) (S)-2-(4-(6-(Benzo[d]thiazol-2-ylmethoxy)pyridin-2-yl)-3-fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    133) (S)-2-(4-(6-((4-Cyano-2-fluorbenzyl)oxy)pyridin-2-yl)-2-methylbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    134) (S)-2-(4-(6-((4-Chlor-2-fluorbenzyl)oxy)pyridin-2-yl)-2-methylbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure, und
    135) (S)-2-(4-(6-(Cyclopropylmethoxy)pyridin-2-yl)-3 -fluorbenzyl)-1-(oxetan-2-ylmethyl)-1H-benzo[d]imidazol-6-carbonsäure,
    oder pharmazeutisch annehmbares Salz davon.
  16. Verbindung nach einem der Ansprüche 1 bis 15 oder pharmazeutisch annehmbares Salz davon zur Verwendung bei Vorbeugung oder Behandlung einer Erkrankung assoziiert mit GLP-1-Aktivität;
    wobei optional die Erkrankung assoziiert mit GLP-1-Aktivität Diabetes, Hyperglykämie, Insulinresistenz, gestörte Glukosetoleranz, diabetische Neuropathie, diabetische Nephropathie, Fettleibigkeit, Glukosestoffwechselstörung, Hyperlipidämie, Dyslipidämie, Herz-Kreislauf-Erkrankung, Arteriosklerose, nichtalkoholische Fettlebererkrankung oder nichtalkoholische Steatohepatitis ist.
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US20230051318A1 (en) 2023-02-16
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